First representative of optically active P-L-menthyl-substituted (aminomethyl)phosphine and its borane and metal complexes

Inorg Chem. 2010 Jun 21;49(12):5407-12. doi: 10.1021/ic902564n.

Abstract

The first representative of 1,5-diaza-3,7-diphosphacyclooctanes (1) with chiral L-menthyl substituents on the phosphorus atoms was obtained by condensation of L-menthylphosphine with formaldehyde and p-toluidine. This optically active cyclic bisphosphine readily forms a stable P,P-complex with borane (2) and P,P-chelate complexes with platinum(II) (3) and palladium(II) dichloride (4). The structure of the bisphosphine 1 in solution was elucidated by employing a variety of 1D/2D NMR correlation experiments, and the molecular structure of complex 3 was studied by X-ray crystallography.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aza Compounds / chemical synthesis*
  • Aza Compounds / chemistry
  • Boranes / chemistry*
  • Crystallography, X-Ray
  • Cyclooctanes / chemical synthesis*
  • Cyclooctanes / chemistry
  • Formaldehyde / chemistry
  • Models, Molecular
  • Molecular Structure
  • Organometallic Compounds / chemistry*
  • Palladium / chemistry*
  • Phosphines / chemistry*
  • Platinum / chemistry*
  • Toluidines / chemistry

Substances

  • 1,5-diaza-3,7-diphosphacyclooctane
  • Aza Compounds
  • Boranes
  • Cyclooctanes
  • Organometallic Compounds
  • Phosphines
  • Toluidines
  • Formaldehyde
  • Platinum
  • Palladium
  • 4-toluidine